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N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis

This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the...

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Autores principales: Boelke, Andreas, Kuczmera, Thomas J., Lork, Enno, Nachtsheim, Boris J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519039/
https://www.ncbi.nlm.nih.gov/pubmed/34160859
http://dx.doi.org/10.1002/chem.202101961
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author Boelke, Andreas
Kuczmera, Thomas J.
Lork, Enno
Nachtsheim, Boris J.
author_facet Boelke, Andreas
Kuczmera, Thomas J.
Lork, Enno
Nachtsheim, Boris J.
author_sort Boelke, Andreas
collection PubMed
description This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the activation of carbon‐ and metal‐chloride bonds as well as carbonyl and nitro groups was achieved. N‐methylated dicationic NHISs rendered the highest reactivity in all investigated catalytic applications with reactivities even higher than all previously described monodentate XB‐donors based on iodine(I) and (III) and the strong Lewis acid BF(3).
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spelling pubmed-85190392021-10-21 N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis Boelke, Andreas Kuczmera, Thomas J. Lork, Enno Nachtsheim, Boris J. Chemistry Communications This article describes the application of N‐heterocyclic iod(az)olium salts (NHISs) as highly reactive organocatalysts. A variety of mono‐ and dicationic NHISs are described and utilized as potent XB‐donors in halogen‐bond catalysis. They were benchmarked in seven diverse test reactions in which the activation of carbon‐ and metal‐chloride bonds as well as carbonyl and nitro groups was achieved. N‐methylated dicationic NHISs rendered the highest reactivity in all investigated catalytic applications with reactivities even higher than all previously described monodentate XB‐donors based on iodine(I) and (III) and the strong Lewis acid BF(3). John Wiley and Sons Inc. 2021-08-05 2021-09-15 /pmc/articles/PMC8519039/ /pubmed/34160859 http://dx.doi.org/10.1002/chem.202101961 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Boelke, Andreas
Kuczmera, Thomas J.
Lork, Enno
Nachtsheim, Boris J.
N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title_full N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title_fullStr N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title_full_unstemmed N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title_short N‐Heterocyclic Iod(az)olium Salts – Potent Halogen‐Bond Donors in Organocatalysis
title_sort n‐heterocyclic iod(az)olium salts – potent halogen‐bond donors in organocatalysis
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519039/
https://www.ncbi.nlm.nih.gov/pubmed/34160859
http://dx.doi.org/10.1002/chem.202101961
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